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rs62620048

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62620048(A;A)
Make rs62620048(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position55470054
GeneWNT5A
is asnp
is mentioned by
dbSNPrs62620048
dbSNP (old)rs62620048
ClinGenrs62620048
ebirs62620048
HLIrs62620048
Exacrs62620048
Varsomers62620048
Maprs62620048
PheGenIrs62620048
Biobankrs62620048
1000 genomesrs62620048
hgdprs62620048
ensemblrs62620048
gopubmedrs62620048
geneviewrs62620048
scholarrs62620048
googlers62620048
pharmgkbrs62620048
gwascentralrs62620048
openSNPrs62620048
23andMers62620048
23andMe allrs62620048
SNP Nexus

SNPshotrs62620048
SNPdbers62620048
MSV3drs62620048
GWAS Ctlgrs62620048
GMAF0.009183
Max Magnitude0

[PMID 23265959] Lack of association of WNT5A mutations with Müllerian duct abnormalities

ClinVar
Risk rs62620048(A;A)
Alt rs62620048(A;A)
Reference Rs62620048(G;G)
Significance Probable-non-pathogenic
Disease Robinow syndrome
Variation info
Gene WNT5A
CLNDBN Robinow syndrome
Reversed 0
HGVS NC_000003.11:g.55504082G>A
CLNSRC
CLNACC RCV000381735.1,